Publication: Effect of prucalopride in the treatment of chronic constipation in Asian and non-Asian women: A pooled analysis of 4 randomized, placebo-controlled studies
dc.contributor.author | Mei Yun Ke | en_US |
dc.contributor.author | Jan Tack | en_US |
dc.contributor.author | Eamonn M.M. Quigley | en_US |
dc.contributor.author | Duowu Zou | en_US |
dc.contributor.author | Suck Chei Choi | en_US |
dc.contributor.author | Somchai Leelakusolvong | en_US |
dc.contributor.author | Andy Liu | en_US |
dc.contributor.author | Jin Yong Kim | en_US |
dc.contributor.other | Peking Union Medical College | en_US |
dc.contributor.other | KU Leuven | en_US |
dc.contributor.other | Methodist Hospital Houston | en_US |
dc.contributor.other | Second Military Medical University | en_US |
dc.contributor.other | Wonkwang University | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Janssen Research and Development | en_US |
dc.contributor.other | Janssen Asia-Pacific | en_US |
dc.date.accessioned | 2018-11-09T03:03:35Z | |
dc.date.available | 2018-11-09T03:03:35Z | |
dc.date.issued | 2014-01-01 | en_US |
dc.description.abstract | © 2014 The Korean Society of Neurogastroenterology and Motility. Background/Aims: To compare the efficacy and safety of prucalopride, a novel selective high-affinity 5-hydroxytryptamine type 4 receptor agonist, versus placebo, in Asian and non-Asian women with chronic constipation (CC). Methods: Data of patients with CC, receiving once-daily prucalopride 2-mg or placebo for 12-weeks, were pooled from 4 double-blind, randomized, phase-III trials (NCT00488137, NCT00483886, NCT00485940 and NCT01116206). The efficacy endpoints were: average of ≥ 3 spontaneous complete bowel movements (SCBMs)/week; average increases of ≥ 1 SCBMs/week; and change from baseline in each CC-associated symptom scores (bloating, abdominal pain, hard stool and straining). Results: Overall, 1,596 women (Asian [26.6%], non-Asian [73.4%]) were included in this analysis. Significantly more patients in the prucalopride group versus placebo experienced an average of ≥ 3 SCBMs/week in Asian (34% vs. 11%, P < 0.001) and non-Asian (24.6% vs. 10.6%, P < 0.001) subgroups. The number of patients reporting an increase of ≥ 1 SCBMs/week from baseline was significantly higher in the prucalopride group versus placebo among both Asian (57.4% vs. 28.3%, P < 0.001) and non-Asian (45.3% vs. 24.0%, P < 0.001) subgroups. The difference between the subgroups was not statistically significant. Prucalopride significantly reduced the symptom scores for bloating, hard stool, and straining in both subgroups. Conclusions: Prucalopride 2-mg once-daily treatment over 12-weeks was more efficacious than placebo in promoting SCBMs and improvement of CC-associated symptoms in Asian and non-Asian women, and was found to be safe and well-tolerated. There were numeric differences between Asian and non-Asian patients on efficacy and treatment emergent adverse events, which may be partially due to the overlap with functional gastrointestinal disorders in non-Asian patients. | en_US |
dc.identifier.citation | Journal of Neurogastroenterology and Motility. Vol.20, No.4 (2014), 458-468 | en_US |
dc.identifier.doi | 10.5056/jnm14029 | en_US |
dc.identifier.issn | 20930887 | en_US |
dc.identifier.issn | 20930879 | en_US |
dc.identifier.other | 2-s2.0-84907577197 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/34811 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84907577197&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | Effect of prucalopride in the treatment of chronic constipation in Asian and non-Asian women: A pooled analysis of 4 randomized, placebo-controlled studies | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84907577197&origin=inward | en_US |